Yunying HE, Hua ZHANG, Ping JI. Effect of TNTs-mediated mitochondrial transfer between mesenchymal stem cells and endothelial cells on vascularization in vitro[J]. Journal of Army Medical University, 2022, 44(4): 310-319.
DOI:
Yunying HE, Hua ZHANG, Ping JI. Effect of TNTs-mediated mitochondrial transfer between mesenchymal stem cells and endothelial cells on vascularization in vitro[J]. Journal of Army Medical University, 2022, 44(4): 310-319. DOI: 10.16016/j.2097-0927.202108167.
Effect of TNTs-mediated mitochondrial transfer between mesenchymal stem cells and endothelial cells on vascularization in vitro
To explore the effect of tunneling nanotubes (TNTs) within mesenchymal stem cells (MSC)/human umbilical vein endothelial cells (HUVEC) co-culture cell spheroids on endothelial cell angiogenesis.
Methods
2
Pre-vascular network formation assay was used to compare the angiogenic ability among the MSC/HUVEC cell spheroid co-culture group
adherent co-culture group
HUVEC 3D culture group and MSC 3D culture group. The expression of β-catenin protein was detected by Western blotting and immunofluorescence staining. The cell spheroids were treated with microfilament depolymerization reagent (CytoD) as a control group
and the above parameters were tested again in the untreated and treated groups. The structure of TNTs was verified by fluorescent labeling and field emission scanning electron microscopy
mitochondrial communication was observed by adenovirus infection
and the mitochondrial status was assessed by mitochondrial membrane potential assay.
Results
2
Compared with the MSC/HUVEC cell spheroid co-culture group
the numbers of junctions and meshes were significantly lower in the adherent co-culture group
HUVEC 3D culture group and MSC 3D culture group (
P
<
0.05). Immunofluorescence staining for β-catenin protein suggested that the spheroid co-culture group had stronger expression than the adherent co-culture group. The results of Western blotting also showed that the intracellular β-catenin expression in the spheroid co-culture group was significantly higher than that in the adherent co-culture group (
P
<
0.05). The presence of TNT (F-actin) between MSC and HUVEC in the co-culture cellular spheroids was shown by phalloidine staining. When the cells were co-cultured as spheroids
the mitochondria derived from HUVEC were observed intracellularly in MSC
and the mitochondria derived from MSC were also observed intracellularly in HUVEC
and the above mitochondrial exchange was diminished in the CytoD-treated group. The mitochondrial membrane potential of the CytoD-treated spheroids was significantly lower than that of the untreated spheroids (
P
<
0.05)
and the proliferation rate and migration range of HUVEC were lower and smaller than those of the untreated spheroids. Compared with the untreated cell spheroid group
the numbers of junctions and meshes were significantly lower in the CytoD-treated cell spheroid group (
P
<
0.05). The total amount of β-catenin protein was significantly higher in the untreated cell spheroid group compared to the CytoD-treated group (
P
<
0.05).
Conclusion
2
Within the co-culture cell spheroids
there are TNTs and their mediated bidirectional mitochondrial transfer between MSC and HUVEC
and they affect the angiogenic ability of HUVEC within these cellular spheroids probably through β-catenin related pathways.
关键词
Keywords
references
CASTRECHINI N M, MURTHI P, GUDE N M, et al . Mesenchymal stem cells in human placental chorionic villi reside in a vascular Niche[J ] . Placenta, 2010, 31(3): 203-212. DOI: 10.1016/j.placenta.2009.12.006.
GRELLIER M, BORDENAVE L, AMÉDÉE J. Cell-to-cell communication between osteogenic and endothelial lineages: implications for tissue engineering[J]. Trends Biotechnol, 2009, 27(10): 562-571. DOI: 10.1016/j.tibtech.2009.07.001.
GRANT P K, SZEP G, PATANGE O, et al . Interpretation of morphogen gradients by a synthetic bistable circuit[J ] . Nat Commun, 2020, 11(1): 5545. DOI: 10.1038/s41467-020-19098-w.
LJUBOJEVIC N, HENDERSON J M, ZURZOLO C. The ways of actin: why tunneling nanotubes are unique cell protrusions[J]. Trends Cell Biol, 2021, 31(2): 130-142. DOI: 10.1016/j.tcb.2020.11.008.
TALBOT J, BRION R, LAMORA A, et al . Connexin43 intercellular communication drives the early differentiation of human bone marrow stromal cells into osteoblasts[J ] . J Cell Physiol, 2018, 233(2): 946-957. DOI: 10.1002/jcp.25938.
JIANG D, CHEN F X, ZHOU H, et al . Bioenergetic crosstalk between mesenchymal stem cells and various ocular cells through the intercellular trafficking of mitochondria[J ] . Theranostics, 2020, 10(16): 7260-7272. DOI: 10.7150/thno.46332.
SISAKHTNEZHAD S, KHOSRAVI L. Emerging physiological and pathological implications of tunneling nanotubes formation between cells[J]. Eur J Cell Biol, 2015, 94(10): 429-443. DOI: 10.1016/j.ejcb.2015.06.010.
MITTAL R, KARHU E, WANG J S, et al . Cell communication by tunneling nanotubes: Implications in disease and thera-peutic applications[J ] . J Cell Physiol, 2019, 234(2): 1130-1146. DOI: 10.1002/jcp.27072.
MURPHY K C, HOCH A I, HARVESTINE J N, et al . Mesenchymal stem cell spheroids retain osteogenic phenotype through α2β1 signaling[J ] . Stem Cells Transl Med, 2016, 5(9): 1229-1237. DOI: 10.5966/sctm.2015-0412.
SEO B J, YOON S H, DO J T. Mitochondrial dynamics in stem cells and differentiation[J]. Int J Mol Sci, 2018, 19(12): E3893. DOI: 10.3390/ijms19123893.
WANG J C, LIU X, QIU Y, et al . Cell adhesio n-mediated mitochondria transfer contributes to mesenchymal stem cell-induced chemoresistance on T cell acute lymphoblastic leukemia cells[J ] . J Hematol Oncol, 2018, 11(1): 11. DOI: 10.1186/s13045-018-0554-z.
BURT R, DEY A, AREF S, et al . Activated stromal cells transfer mitochondria to rescue acute lymphoblastic leukemia cells from oxidative stress[J ] . Blood, 2019, 134(17): 1415-1429. DOI: 10.1182/blood.2019001398.
SINCLAIR K A, YERKOVICH S T, HOPKINS P M, et al . Characterization of intercellular communication and mitochondrial donation by mesenchymal stromal cells derived from the human lung[J ] . Stem Cell Res Ther, 2016, 7(1): 91. DOI: 10.1186/s13287-016-0354-8.
JIANG L, YIN M, XU J, et al . The transcription factor Bach1 suppresses the developmental angiogenesis of zebrafish[J ] . Oxid Med Cell Longev, 2017, 2017: 2143875. DOI: 10.1155/2017/2143875.
FOURNIER P, VIALLARD C, DEJDA A, et al . The protein tyrosine phosphatase PTPRJ/DEP-1 contributes to the regulation of the Notch-signaling pathway and sprouting angiogenesis[J ] . Angiogenesis, 2020, 23(2): 145-157. DOI: 10.1007/s10456-019-09683-z.
YI C, WU W, ZHENG D, et al . Targeted inhibition of endo thelial calpain delays wound healing by reducing inflammation and angiogenesis[J ] . Cell Death Dis, 2020, 11(7): 533. DOI: 10.1038/s41419-020-02737-x.
ZHANG J L, WHITEHEAD J, LIU Y, et al . Direct observation of tunneling nanotubes within human mesenchymal stem cell spheroids[J ] . J Phys Chem B, 2018, 122(43): 9920-9926. DOI: 10.1021/acs.jpcb.8b07305.
NAJDANOVIĆ J G, CVETKOVIĆ V J, STOJANOVIĆ S T, et al . Vascularization and osteogenesis in ectopically implanted bone tissue-engineered constructs with endothelial and osteogenic differentiated adipose-derived stem cells[J ] . World J Stem Cells, 2021, 13(1): 91-114. DOI: 10.4252/wjsc.v13.i1.91.
WANG L, ZHU L X, WANG Z, et al . Development of a centrally vascularized tissue engineering bone graft with the unique core-shell composite structure for large femoral bone defect treatment[J ] . Biomaterials, 2018, 175: 44-60. DOI: 10.1016/j.biomaterials.2018.05.017.
HEO D N, HOSPODIUK M, OZBOLAT I T. Synergistic interplay between human MSCs and HUVECs in 3D spheroids laden in collagen/fibrin hydrogels for bone tissue engineering[J]. Acta Biomater, 2019, 95: 348-356. DOI: 10.1016/j.actbio.2019.02.046.
ZHANG J, NEOH K G, KANG E T. Electrical stimulation of adipose-derived mesenchymal stem cells and endothelial cells co-cultured in a conductive scaffold for potential orthopaedic applications[J]. J Tissue Eng Regen Med, 2018, 12(4): 878-889. DOI: 10.1002/term.2441.
MAHON O R, BROWE D C, GONZALEZ-FERNANDEZ T, et al . Nano-particle mediated M2 macrophage polarization enhances bone formation and MSC osteogenesis in an IL-10 dependent manner[J ] . Biomaterials, 2020, 239: 119833. DOI: 10.1016/j.biomaterials.2020.119833.
TODA S, FRANKEL N W, LIM W A. Engineering cell-cell communication networks: programming multicellular behaviors[J]. Curr Opin Chem Biol, 2019, 52: 31-38. DOI: 10.1016/j.cbpa.2019.04.020.
SONG Z Y, WANG F, CUI S X, et al . Knockdown of CXCR4 inhibits CXCL12-induced angiogenesis in HUVECs through downregulation of the MAPK/ERK and PI3K/AKT and the wnt/β-catenin pathways[J ] . Cancer Invest, 2018, 36(1): 10-18. DOI: 10.1080/07357907.2017.1422512.
SHEN M, BAI D, LIU B, et al . Dysregulated Txnip-ROS-Wnt axis contributes to the impaired ischemic heart repair in diabetic mice[J ] . Biochim Biophys Acta Mol Basis Dis, 2018, 1864(12): 3735-3745. DOI: 10.1016/j.bbadis.2018.09.029.
QIU J J, SUN S G, TANG X Y, et al . Extracellular vesicular Wnt7b mediates HPV E6-induced cervical cancer angiogenesis by activating the β-catenin signaling pathway[J ] . J Exp Clin Cancer Res, 2020, 39(1): 260. DOI: 10.1186/s13046-020-01745-1.
RATUSHNYY A, EZDAKOVA M, BURAVKOVA L. Secretome of senescent adipose-derived mesenchymal stem cells negatively regulates angiogenesis[J]. Int J Mol Sci, 2020, 21(5): 1802. DOI: 10.3390/ijms21051802.
YU M Y, LIU W, LI J X, et al . Exosomes derived from atorvastatin-pretreated MSC accelerate diabetic wound repair by enhancing angiogenesis via AKT/ENOS pathway[J ] . Stem Cell Res Ther, 2020, 11(1): 350. DOI: 10.1186/s13287-020-01824-2..
FENG Y H, ZHU R J, SHEN J, et al . Human bone marrow mesenchymal stem cells rescue endothelial cells experiencing chemotherapy stress by mitochondrial transfer via tunneling nanotubes[J ] . Stem Cells Dev, 2019, 28(10): 674-682. DOI: 10.1089/scd.2018.0248..
ISLAM M N, DAS S R, EMIN M T, et al . Mitochondrial transfer from bone-marrow-derived stromal cells to pulmonary alveoli protects against acute lung injury[J ] . Nat Med, 2012, 18(5): 759-765. DOI: 10.1038/nm.2736.
ACQUISTAPACE A, BRU T, LESAULT P F, et al . Human mesenchymal stem cells reprogram adult cardiomyocytes toward a progenitor-like state through partial cell fusion and mitochondria transfer[J ] . Stem Cells, 2011, 29(5): 812-824. DOI: 10.1002/stem.632.
GUO Y S, CHI X P, WANG Y F, et al . Mitochondria transfer enhances proliferation, migration, and osteogenic differentiation of bone marrow mesenchymal stem cell and promotes bone defect healing[J ] . Stem Cell Res Ther, 2020, 11(1): 245. DOI: 10.1186/s13287-020-01704-9.
Mitochondrial transfer from neural stem cells rescues apoptosis of retinal pigment epithelial cells isolated from RCS rats
Chronic hypoxia reduces cold tolerance via hepatic ANGPTL3-driven mitochondrial damage and adipose thermogenesis suppression
Translocator protein promotes renal angiotensin Ⅱ type 1 receptor expression and increases blood pressure in spontaneously hypertensive rats
Ethacrynic acid promotes apoptosis in lung cancer A549 cells when combined with cisplatin chemotherapy
Effect of cervical sympathetic ganglia block on hippocampal mitochondria in diabetic rats
Related Author
陈冲林
邹婷
黎其友
徐海伟
阴正勤
HUANG Yujie
HUANG Lingfang
ZHEGN Minghai
Related Institution
Department of Clinical Nursing, School of Nursing, Army Medical University (Third Military Medical University)
Key Laboratory of Extreme Environmental Medicine of Ministry of Education, School of Nursing, Army Medical University (Third Military Medical University)
Department of Frigid Zone Medicine, College of High Altitude Military Medicine, School of Nursing, Army Medical University (Third Military Medical University)
Department of Internal Medicine, Hospital of Troop 95877
Department of Cardiology, Chongqing Institute of Cardiology, Institute of Surgery Research, Third Affiliated Hospital, Army Medical University (Third Military Medical University)